All Study Guides Microbiology Unit 17
🦠 Microbiology Unit 17 – Innate Nonspecific Host DefensesInnate immunity is our body's first line of defense against pathogens. It includes physical barriers like skin, chemical barriers like stomach acid, and cellular components like phagocytes. These defenses work together to prevent infection and activate adaptive immunity when needed.
The innate immune system responds quickly but non-specifically to threats. It includes the inflammatory response, which helps localize and eliminate pathogens. Key players are phagocytes, dendritic cells, natural killer cells, and the complement system, which enhance pathogen clearance.
Key Concepts and Definitions
Innate immunity provides immediate, non-specific defense against pathogens and foreign substances
Consists of physical barriers, chemical barriers, and cellular components that work together to prevent infection
Innate immune responses are genetically determined and do not require prior exposure to a pathogen
Includes the inflammatory response, which is a complex series of events that helps to localize and eliminate pathogens
Key cells involved in innate immunity include phagocytes (neutrophils and macrophages), dendritic cells, and natural killer cells
The complement system is a group of plasma proteins that enhance the ability of antibodies and phagocytic cells to clear pathogens
Innate immunity is the first line of defense against infection and plays a crucial role in activating adaptive immunity
Types of Innate Defenses
Physical barriers include the skin, mucous membranes, and other mechanical barriers that prevent the entry of pathogens
Chemical barriers consist of enzymes, acids, and antimicrobial peptides that create an inhospitable environment for pathogens
Examples include lysozyme in tears and saliva, low pH of the stomach, and defensins in the intestinal tract
Cellular components involve various immune cells that recognize and respond to pathogens
Phagocytes (neutrophils and macrophages) engulf and destroy pathogens
Dendritic cells capture, process, and present antigens to T cells, linking innate and adaptive immunity
Natural killer cells destroy virus-infected and tumor cells without prior sensitization
The inflammatory response is a complex cascade of events that helps to localize and eliminate pathogens
The complement system enhances the ability of antibodies and phagocytic cells to clear pathogens
Physical and Chemical Barriers
The skin is the largest organ and serves as a physical barrier against pathogens
Keratinocytes produce keratin, which forms a tough, waterproof layer
Langerhans cells in the epidermis capture and present antigens to T cells
Mucous membranes line the respiratory, digestive, and urogenital tracts and secrete mucus, which traps pathogens
Cilia in the respiratory tract sweep mucus and trapped particles out of the lungs
Tears, saliva, and other secretions contain lysozyme, an enzyme that breaks down bacterial cell walls
The low pH of the stomach creates an acidic environment that kills many ingested pathogens
Defensins are antimicrobial peptides found in the intestinal tract, respiratory tract, and skin
They create pores in bacterial cell membranes, leading to cell lysis
Urine flow and vaginal secretions help to mechanically remove pathogens from the urogenital tract
Cellular Components of Innate Immunity
Phagocytes are cells that engulf and destroy pathogens
Neutrophils are the most abundant type of white blood cell and are the first to respond to infection
Macrophages are long-lived cells that reside in tissues and continue to fight infection after neutrophils have died
Dendritic cells are specialized antigen-presenting cells that capture, process, and present antigens to T cells
They link innate and adaptive immunity by activating T cells and initiating an adaptive immune response
Natural killer (NK) cells are lymphocytes that destroy virus-infected and tumor cells without prior sensitization
They release cytotoxic granules containing perforin and granzymes, which induce apoptosis in target cells
Eosinophils are granulocytes that defend against parasitic infections and play a role in allergic responses
Basophils and mast cells release histamine and other mediators that contribute to inflammation and allergic reactions
Inflammatory Response
Inflammation is a complex cascade of events that helps to localize and eliminate pathogens
Triggered by tissue damage or infection, which causes the release of inflammatory mediators (cytokines, chemokines, and prostaglandins)
Vasodilation increases blood flow to the affected area, causing redness and heat
Increased vascular permeability allows fluid and immune cells to enter the tissue, causing swelling
Pain results from the stimulation of nerve endings by inflammatory mediators
Neutrophils are the first cells to arrive at the site of inflammation, followed by macrophages
They phagocytose pathogens and release additional inflammatory mediators
The inflammatory response helps to localize the infection, prevent the spread of pathogens, and promote tissue repair
Chronic inflammation can contribute to the development of diseases such as atherosclerosis, cancer, and autoimmune disorders
Complement System
The complement system is a group of plasma proteins that enhance the ability of antibodies and phagocytic cells to clear pathogens
Consists of three activation pathways: classical, alternative, and lectin pathways
The classical pathway is activated by antibody-antigen complexes
The alternative pathway is activated by microbial surfaces and does not require antibodies
The lectin pathway is activated by the binding of mannose-binding lectin to microbial carbohydrates
All three pathways converge on the formation of C3 convertase, which cleaves C3 into C3a and C3b
C3b opsonizes pathogens, enhancing phagocytosis by macrophages and neutrophils
The terminal pathway leads to the formation of the membrane attack complex (MAC), which creates pores in the pathogen's cell membrane, causing lysis
Complement activation also generates anaphylatoxins (C3a and C5a), which promote inflammation and recruit immune cells to the site of infection
Innate vs. Adaptive Immunity
Innate immunity is the first line of defense against pathogens and provides immediate, non-specific protection
Adaptive immunity is a slower, more specific response that develops after exposure to a pathogen
Innate immunity does not confer long-lasting protection, while adaptive immunity provides immunological memory
Innate immune responses are genetically determined, while adaptive immune responses are acquired through exposure to antigens
Innate immunity involves physical barriers, chemical barriers, and cellular components (phagocytes, dendritic cells, and NK cells)
Adaptive immunity involves T lymphocytes and B lymphocytes, which produce specific antibodies and cell-mediated responses
Innate immunity plays a crucial role in activating adaptive immunity through antigen presentation by dendritic cells
Clinical Relevance and Applications
Deficiencies in innate immune components can lead to increased susceptibility to infections
Chronic granulomatous disease is caused by defects in phagocyte oxidative burst, leading to recurrent bacterial and fungal infections
Leukocyte adhesion deficiency is caused by defects in neutrophil adhesion and migration, resulting in recurrent soft tissue infections
Excessive or inappropriate activation of innate immunity can contribute to inflammatory and autoimmune diseases
Rheumatoid arthritis is characterized by chronic inflammation of the joints, mediated by innate immune cells and cytokines
Inflammatory bowel disease (Crohn's disease and ulcerative colitis) involves dysregulated innate immune responses in the gut
Targeting innate immune pathways is a promising approach for the development of new therapies
Toll-like receptor (TLR) agonists are being investigated as vaccine adjuvants and cancer immunotherapies
Complement inhibitors are being developed for the treatment of inflammatory and autoimmune diseases
Understanding the interplay between innate and adaptive immunity is crucial for the development of effective vaccines and immunotherapies